U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 238

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142909copy number variation1nstd232human GRCh37.p13 chr1: 160,969,537-160,969,664 , GRCh38.p12 chr1: 160,999,747-160,999,874 F11R
    nsv7099240copy number variation1nstd231human GRCh38.p12 chr1: 159,722,599-161,418,916 , GRCh37 chr1: 159,692,389-161,388,706 APOA2, ATP1A2, 87 more genes
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7041046inversion1nstd229human GRCh38 chr1: 160,990,161-160,996,895 , GRCh37.p13 chr1: 160,959,951-160,966,685 F11R
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643369copy number variation1nstd229human GRCh38 chr1: 161,007,090-161,007,288 , GRCh37.p13 chr1: 160,976,880-160,977,078 F11R
    nsv6643274copy number variation1nstd229human GRCh38 chr1: 160,990,054-160,996,363 , GRCh37.p13 chr1: 160,959,844-160,966,153 F11R
    nsv6643148copy number variation1nstd229human GRCh38 chr1: 161,003,725-161,006,182 , GRCh37.p13 chr1: 160,973,515-160,975,972 F11R
    nsv6643147copy number variation1nstd229human GRCh38 chr1: 160,993,643-160,996,938 , GRCh37.p13 chr1: 160,963,433-160,966,728 F11R
    nsv6636729copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,778,879-161,190,622 , GRCh38.p12 chr1: 160,809,089-161,220,832 CD244, LOC646347, 24 more genes
    nsv6333959copy number variation1nstd223human GRCh38 chr1: 160,993,642-160,996,937 , GRCh37.p13 chr1: 160,963,432-160,966,727 F11R
    nsv6332269copy number variation1nstd223human GRCh38 chr1: 160,388,767-162,811,116 , GRCh37.p13 chr1: 160,358,557-162,780,906 ATF6-DT, RPS23P10, 119 more genes
    nsv6322385copy number variation1nstd223human GRCh38 chr1: 161,009,708-161,010,203 , GRCh37.p13 chr1: 160,979,498-160,979,993 F11R
    nsv6320212copy number variation1nstd223human GRCh38 chr1: 160,991,374-160,994,900 , GRCh37.p13 chr1: 160,961,164-160,964,690 F11R
    nsv6319516copy number variation1nstd223human GRCh38 chr1: 161,007,090-161,007,288 , GRCh37.p13 chr1: 160,976,880-160,977,078 F11R
    nsv6313604copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805 USF1, TRE-CTC1-3, 161 more genes
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6296795copy number variation1nstd186human GRCh37 chr1: 160,986,377-161,000,377 , GRCh38.p12 chr1: 161,016,587-161,030,587 F11R
    nsv6292597mobile element insertion1nstd186human GRCh37 chr1: 160,989,783-160,989,793 , GRCh38.p12 chr1: 161,019,993-161,020,003 F11R
    nsv6290394copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 160,859,558-161,409,185 , GRCh38.p12 chr1: 160,889,768-161,439,395 APOA2, FCER1G, 39 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center